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16
Angiogenesis
Bcr-Abl
BTK
EGFR
FAK
FGFR
FLT3
HIF
JAK
PDGFR
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Syk
VDA
VEGFR
Bcl-2
test3
demo333
8
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2
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9
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11
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8
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Topoisomerase
5-alpha Reductase
8
Endocrinology & Hormones
Androgen Receptor
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Estrogen/progestogen Receptor
Glucocorticoid Receptor
GPR
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12
Epigenetics
DNA Methyltransferase
Epigenetic Reader Domain
HDAC
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Histone Acetyltransferase
Histone Demethylase
Histone Methyltransferase
JAK
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Pim
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19
GPCR & G Protein
Adenosine Receptor
Adrenergic Receptor
cAMP
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CXCR
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OX Receptor
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EGFR
4
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STAT
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5
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10
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20
Metabolism
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5
Microbiology
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17
Neuronal Signaling
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4
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9
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9
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16
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EGFR
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8
Stem Cells / Wnt
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Bcr-Abl
4
TGF-beta /Smad
KC
ROCK
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DUB
5
Ubiquitin
E1 Activating
E2 Conjugating
E3 Ligase
p97
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2
Lipid reagent
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2
Photodynamic therapy
Photodynamic Therapy (PDT)
Porphyrin
EGFR Products
or product name starting with:
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H100490A
Lapatinib (free base)
featured
Lapatinib is a synthetic, orally-active quinazoline with potential antineoplastic activity. Lapatini…
H200298
Sapitinib free base
featured
Sapitinib, also known as AZD-8931, is an erbB receptor tyrosine kinase inhibitor with potential anti…
H205669
Capivasertib
featured
AZD5363, also known as Capivasertib, is an orally available inhibitor of the serine/threonine protei…
H406106
CL-387785
featured
CL-387785, also known as EKI-785 , is a n irreversible inhibitor of EGF-receptor (EGFR) kinase activ…
H203170
WZ4002
featured
WZ4002 is EGFR inhibitor against EGFR T790M (mutation of the gatekeeper T790 residue) which is dete…
H406396
UNC2250
featured
UNC2250 is a potent and selective Mer Kinase inhibitor. When applied to live cells, UNC2250 inhibite…
H205765
Brigatinib-analog
featured
Brigatinib-analog is an orally active, potent and selective anaplastic lymphoma kinase (ALK) and th…
H406653
FIIN-3
new
featured
FIIN-3 is a potent, selective, irreversible and the next-generation covalent FGFR inhibitor. FIIN-3 …
H406651
DW532
DW532 is one of simplified analogues of hematoxylin that has shown broad-spectrum inhibition on tyro…
H406121
WHI-P154
featured
WHI-P154 is a JAK3 inhibitor with IC50 = 1.8 microM. WHI-P154 displays no activity at JAK1 or JAK2. …
H205660
Varlitinib
featured
Varlitinib, also known as ARRY-543 and ASLAN001, is an orally bioavailable inhibitor of the epiderma…
H558308
Vandetanib
featured
Vandetanib is an orally bioavailable 4-anilinoquinazoline. Vandetanib selectively inhibits the tyros…
H205494
Capmatinib
featured
Capmatinib, also known as INCB28060 and INC280, is an orally bioavailable inhibitor of the proto-onc…
H205847
Icotinib HCl
featured
Icotinib, also known as BPI-2009, is an orally available quinazoline-based inhibitor of epidermal gr…
H205487
HSP-990
featured
HSP990 is an orally bioavailable inhibitor of human heat-shock protein 90 (Hsp90) with potential ant…
H201072
Golvatinib
featured
Golvatinib, also known as E7050, is an orally bioavailable dual kinase inhibitor of c-Met (hepatocyt…
H202703
Ganetespib (STA-9090)
featured
Ganetespib, also known as STA-9090, is a synthetic small-molecule inhibitor of heat shock protein 90…
H205576
Dacomitinib
featured
Dacomitinib, also known as PF-299 and PF-00299804 ; or PF299804, is an orally bioavailable, highly s…
H205796
Rociletinib
featured
Rociletinib, also known as AVL-301 and CO1686, is an orally available small molecule, irreversible i…
H120204
Afatinib dimaleate
featured
Afatinib dimaleate is an orally bioavailable dual receptor tyrosine kinase (RTK) inhibitor with pote…
H200078
AC480 HCl
featured
AC480, also known as BMS-599626, is an orally bioavailable inhibitor of the HER1, HER2 and HER4 tyro…
H100946
Lapatinib ditosylate
featured
Lapatinib is a synthetic, orally-active quinazoline with potential antineoplastic activity. Lapatini…
H206042
Osimertinib free base
featured
Osimertinib, also known as AZD-9291 and Mereletinib, is a third-generation EGFR inhibitor, showed pr…
H100140
Gefitinib
featured
Gefitinib, also known as ZD1839, is an anilinoquinazoline with antineoplastic activity. Gefitinib in…
H100300
Erlotinib hydrochloride
featured
Erlotinib hydrochloride is the hydrochloride salt of a quinazoline derivative with antineoplastic pr…
H201913
MK-2206 2HCl
featured
MK2206 is a Akt inhibitor, is also an orally bioavailable allosteric inhibitor of the serine/threoni…
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